Service de Biostatistique et d'Epidémiologie, Institut Gustave Roussy, Villejuif, France.
Stat Med. 2011 Jun 15;30(13):1584-94. doi: 10.1002/sim.4128. Epub 2011 Feb 24.
We propose a hybrid design, the time-to-event dose-escalation method with overdose control (TITE-EWOC), introducing the time-to-event approach, developed by Cheungit et al., in the EWOC method, developed by Babb et al. The aim of this new design is to decrease the dose-finding trial duration, without impairing the characteristics of the EWOC design, especially the overdose control ability. We conducted a simulation study, exploring four dose–toxicity relationships and three mean inter-patient arrival times. Performances of TITE-EWOC were compared with those of the EWOC method. This study shows that the trial duration can be greatly decreased with the TITE-EWOC, without impacting the proportion of overdosed patients or the number of dose-limiting toxicities by trial, for all explored dose–toxicity relationships, except for very short inter-patient arrival times. The ability of the method to find the true maximum tolerated dose remains unchanged.
我们提出了一种混合设计,即时间事件剂量递增法与过度控制(TITE-EWOC),在 Babb 等人开发的 EWOC 方法中引入了 Cheungit 等人开发的时间事件方法。这种新设计的目的是在不损害 EWOC 设计特征的情况下,特别是过度控制能力,缩短剂量发现试验的持续时间。我们进行了一项模拟研究,探索了四种剂量-毒性关系和三种平均患者间到达时间。比较了 TITE-EWOC 与 EWOC 方法的性能。这项研究表明,对于所有探索的剂量-毒性关系,除了非常短的患者间到达时间外,TITE-EWOC 可以大大缩短试验持续时间,而不会影响过度用药患者的比例或试验中剂量限制毒性的数量。该方法确定真实最大耐受剂量的能力保持不变。